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IRMM316

Nivalenol in acetonitrile

IRMM®, certified reference material

Synonym(s):

Nivalenol solution, 3α,4β,7α, 15-Tetrahydroxy-12,13-epoxytrichothec-9-en-8-one, NIV

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$330.00

About This Item

Empirical Formula (Hill Notation):
C15H20O7
CAS Number:
23282-20-4
Molecular Weight:
312.32
EC Number:
200-835-2
MDL number:
MFCD00133673
UNSPSC Code:
41116107
PubChem Substance ID:
329815694
NACRES:
NA.24

$330.00

PRICE WITHOUT NATIONAL TAXES
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Request a Bulk Order

grade

certified reference material

Agency

IRMM®

manufacturer/tradename

JRC

application(s)

general analytical

format

matrix material

SMILES string

[H][C@]12O[C@]3([H])[C@H](O)[C@@H](O)[C@@](C)([C@]34CO4)[C@@]1(CO)[C@H](O)C(=O)C(C)=C2

InChI

1S/C15H20O7/c1-6-3-7-14(4-16,11(20)8(6)17)13(2)10(19)9(18)12(22-7)15(13)5-21-15/h3,7,9-12,16,18-20H,4-5H2,1-2H3/t7-,9-,10-,11-,12-,13-,14-,15+/m1/s1

InChI key

UKOTXHQERFPCBU-XBXCNEFVSA-N

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This Item
IRMM31534131CRM46911
Nivalenol in acetonitrile IRMM®, certified reference material

IRMM316

Nivalenol in acetonitrile

4-Deoxynivalenol in acetonitrile IRMM®, certified reference material

IRMM315

4-Deoxynivalenol in acetonitrile

Nivalenol solution 100 μg/mL in acetonitrile, analytical standard

34131

Nivalenol solution

Deoxynivalenol solution certified reference material, 200 μg/mL in ethyl acetate: methanol (95:5), ampule of 1 mL

CRM46911

Deoxynivalenol solution

format

matrix material

format

matrix material

format

single component solution

format

single component solution

grade

certified reference material

grade

certified reference material

grade

analytical standard

grade

certified reference material, TraceCERT®

manufacturer/tradename

JRC

manufacturer/tradename

JRC

manufacturer/tradename

-

manufacturer/tradename

-

agency

IRMM®

agency

IRMM®

agency

-

agency

-

Analysis Note

For more information please see:
IRMM316

Legal Information

IRMM is a registered trademark of European Commission

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

35.6 °F - closed cup

Flash Point(C)

2.0 °C - closed cup

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E D Van Asselt et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 29(10), 1556-1565 (2012-06-30)
Mycotoxins are secondary metabolites produced by fungi that can cause adverse health effects. Due to climate change, temperatures are expected to rise and changes in rainfall patterns are foreseen. These developments may increase fungal occurrence and mycotoxin concentrations in maize.
G Barros et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 29(2), 293-303 (2011-05-21)
Soybean (Glycine max L.), the main source of protein throughout the world, is used both as a food and a feedstuff. Currently, limited information about the occurrence of Fusarium species and mycotoxins in soybean grain and by-products is available. The
Matias Pasquali et al.
Electrophoresis, 34(4), 505-509 (2012-11-23)
Fusarium graminearum is widely studied as a model for toxin production among plant pathogenic fungi. A 2D DIGE reference map for the nivalenol-producing strain 453 was established. Based on a whole protein extract, all reproducible spots were systematically picked and
Marilena Muscarella et al.
Talanta, 97, 145-149 (2012-07-31)
A rapid, sensitive and selective analytical method was developed for the quantitative determination of deoxynivalenol (DON) and nivalenol (NIV) in cereals intended for human and animal consumption. The method, based on liquid chromatography and fluorescence detection, involves an automated 2
Tadahiro Suzuki et al.
Journal of agricultural and food chemistry, 60(37), 9519-9527 (2012-08-18)
Type B trichothecenes, deoxynivalenol (DON) and nivalenol (NIV), are secondary metabolites of Fusarium species and are major pollutants in food and feed products. Recently, the production trend of their derivatives, 3-acetyldeoxynivalenol (3-AcDON), 15-acetyldeoxynivalenol (15-AcDON), and 4-acetylnivalenol (4-AcNIV or fusarenon-X), has
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